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New clinical and biological insights from the international TARGIT-A randomised trial of targeted intraoperative radiotherapy during lumpectomy for breast cancer.
Vaidya, Jayant S; Bulsara, Max; Baum, Michael; Wenz, Frederik; Massarut, Samuele; Pigorsch, Steffi; Alvarado, Michael; Douek, Michael; Saunders, Christobel; Flyger, Henrik; Eiermann, Wolfgang; Brew-Graves, Chris; Williams, Norman R; Potyka, Ingrid; Roberts, Nicholas; Bernstein, Marcelle; Brown, Douglas; Sperk, Elena; Laws, Siobhan; Sütterlin, Marc; Corica, Tammy; Lundgren, Steinar; Holmes, Dennis; Vinante, Lorenzo; Bozza, Fernando; Pazos, Montserrat; Blanc-Onfroy, Magali Le; Gruber, Günther; Polkowski, Wojciech; Dedes, Konstantin J; Niewald, Marcus; Blohmer, Jens; McReady, David; Hoefer, Richard; Kelemen, Pond; Petralia, Gloria; Falzon, Mary; Joseph, David; Tobias, Jeffrey S.
Afiliação
  • Vaidya JS; Division of Surgery and Interventional Science, University College London, London, UK. jayantvaidya@gmail.com.
  • Bulsara M; Department of Biostatistics, University of Notre Dame, Fremantle, WA, Australia.
  • Baum M; Division of Surgery and Interventional Science, University College London, London, UK.
  • Wenz F; Department of Radiation Oncology, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Massarut S; Department of Surgery, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.
  • Pigorsch S; Department of Radiation Oncology, Red Cross Hospital, Technical University of Munich, Munich, Germany.
  • Alvarado M; Department of Surgery, University of California, San Francisco, CA, USA.
  • Douek M; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
  • Saunders C; School of Surgery, University of Western Australia, Perth, WA, Australia.
  • Flyger H; Department of Breast Surgery, University of Copenhagen, Copenhagen, Denmark.
  • Eiermann W; Department of Gynecology and Obstetrics, Red Cross Hospital, Technical University of Munich, Munich, Germany.
  • Brew-Graves C; Division of Surgery and Interventional Science, University College London, London, UK.
  • Williams NR; Division of Surgery and Interventional Science, University College London, London, UK.
  • Potyka I; Division of Surgery and Interventional Science, University College London, London, UK.
  • Roberts N; Division of Surgery and Interventional Science, University College London, London, UK.
  • Bernstein M; Patient advocate and writer, London, UK.
  • Brown D; Department of Surgery, Ninewells Hospital, Dundee, UK.
  • Sperk E; Department of Radiation Oncology, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Laws S; Department of Surgery, Royal Hampshire County Hospital, Winchester, UK.
  • Sütterlin M; Department of Gynecology and Obstetrics, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, Berlin, Germany.
  • Corica T; Department of Radiation Oncology, Sir Charles Gairdner Hospital, Perth, WA, Australia.
  • Lundgren S; Department of Oncology, St Olav's University Hospital, & Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
  • Holmes D; John Wayne Cancer Institute & Helen Rey Breast Cancer Foundation, University of Southern California, Los Angeles, CA, USA.
  • Vinante L; Department of Radiation Oncology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.
  • Bozza F; Department of Surgery, Instituto Oncologico Veneto (IVO) IRCCS, Padoa, Italy.
  • Pazos M; Department of Radiation Oncology, University Hospital, Ludwig Maximilians Universitat, Munich, Germany.
  • Blanc-Onfroy ML; Oncologie radiothérapeute, Institut de Cancérologie de l'Ouest, Nantes, France.
  • Gruber G; Brust Zentrum Seefeld, Zurich, Switzerland.
  • Polkowski W; Department of Surgical Oncology, Medical University of Lublin, Lublin, Poland.
  • Dedes KJ; Breast Center, Universitätsspital Zürich, Zurich, Switzerland.
  • Niewald M; Saarland University Medical Center, Homburg, Germany.
  • Blohmer J; Sankt Gertrauden-Krankenhaus, and The Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • McReady D; Princess Margaret Cancer Centre, Toronto, Canada.
  • Hoefer R; Sentara Surgery Specialists, Hampton, VA, USA.
  • Kelemen P; Ashikari Breast Center, New York Medical College, New York, NY, USA.
  • Petralia G; Department of Surgery, University College London Hospitals, London, UK.
  • Falzon M; Department of Pathology University College London Hospitals, London, UK.
  • Joseph D; Department of Radiation Oncology, Sir Charles Gairdner Hospital, Perth, WA, Australia.
  • Tobias JS; Department of Clinical Oncology, University College London Hospitals, London, UK.
Br J Cancer ; 125(3): 380-389, 2021 08.
Article em En | MEDLINE | ID: mdl-34035435
ABSTRACT

BACKGROUND:

The TARGIT-A trial reported risk-adapted targeted intraoperative radiotherapy (TARGIT-IORT) during lumpectomy for breast cancer to be as effective as whole-breast external beam radiotherapy (EBRT). Here, we present further detailed analyses.

METHODS:

In total, 2298 women (≥45 years, invasive ductal carcinoma ≤3.5 cm, cN0-N1) were randomised. We investigated the impact of tumour size, grade, ER, PgR, HER2 and lymph node status on local recurrence-free survival, and of local recurrence on distant relapse and mortality. We analysed the predictive factors for recommending supplemental EBRT after TARGIT-IORT as part of the risk-adapted approach, using regression modelling. Non-breast cancer mortality was compared between TARGIT-IORT plus EBRT vs. EBRT.

RESULTS:

Local recurrence-free survival was no different between TARGIT-IORT and EBRT, in every tumour subgroup. Unlike in the EBRT arm, local recurrence in the TARGIT-IORT arm was not a predictor of a higher risk of distant relapse or death. Our new predictive tool for recommending supplemental EBRT after TARGIT-IORT is at https//targit.org.uk/addrt . Non-breast cancer mortality was significantly lower in the TARGIT-IORT arm, even when patients received supplemental EBRT, HR 0.38 (95% CI 0.17-0.88) P = 0.0091.

CONCLUSION:

TARGIT-IORT is as effective as EBRT in all subgroups. Local recurrence after TARGIT-IORT, unlike after EBRT, has a good prognosis. TARGIT-IORT might have a beneficial abscopal effect. TRIAL REGISTRATION ISRCTN34086741 (21/7/2004), NCT00983684 (24/9/2009).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Mastectomia Segmentar / Carcinoma Ductal de Mama Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Mastectomia Segmentar / Carcinoma Ductal de Mama Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido